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将非化学计量比的NiSe与MoSe耦合于碳空心纳米花中以实现对锂氧电池的高效电催化协同效应。

Coupling MoSe with Non-Stoichiometry Ni Se in Carbon Hollow Nanoflowers for Efficient Electrocatalytic Synergistic Effect on Li-O Batteries.

作者信息

Long Yuxin, Li Qiang, Zhang Zidong, Zeng Qingxi, Liu Dong, Zhao Lanling, Liu Yao, Li Yebing, Zhang Yiming, Ji Kunqian, Zhou Zhaorui, Han Xue, Wang Jun

机构信息

Key Laboratory for Liquid-Solid Structural Evolution and Processing of Materials (Ministry of Education), Shandong University, Jinan, 250061, China.

Shandong Tianhou New Material Technology Co. Ltd., Heze, 274051, China.

出版信息

Small. 2024 Mar;20(10):e2304882. doi: 10.1002/smll.202304882. Epub 2023 Oct 27.

DOI:10.1002/smll.202304882
PMID:37890468
Abstract

Li-O batteries could deliver ultra-high theoretical energy density compared to current Li-ion batteries counterpart. The slow cathode reaction kinetics in Li-O batteries, however, limits their electrocatalytic performance. To this end, MoSe and Ni Se nanoflakes were decorated in carbon hollow nanoflowers, which were served as the cathode catalysts for Li-O batteries. The hexagonal Ni Se and MoSe show good structural compatibility with the same space group, resulting in a stable heterogeneous structure. The synergistic interaction of the unsaturated atoms and the built-in electric fields on the heterogeneous structure exposes abundant catalytically active sites, accelerating ion and charge transport and imparting superior electrochemical activity, including high specific capacities and stable cycling performance. More importantly, the lattice distances of the Ni Se (101) plane and MoSe (100) plane at the heterogeneous interfaces are highly matched to that of Li O (100) plane, facilitating epitaxial growth of Li O , as well as the formation and decomposition of discharge products during the cycles. This strategy of employing nonstoichiometric compounds to build heterojunctions and improve Li-O battery performance is expected to be applied to other energy storage or conversion systems.

摘要

与目前的锂离子电池相比,锂氧电池可以提供超高的理论能量密度。然而,锂氧电池中缓慢的阴极反应动力学限制了它们的电催化性能。为此,硒化钼和硒化镍纳米片被修饰在碳空心纳米花中,作为锂氧电池的阴极催化剂。六方晶系的硒化镍和硒化钼与相同的空间群表现出良好的结构相容性,形成了稳定的异质结构。异质结构上不饱和原子与内建电场的协同相互作用暴露出丰富的催化活性位点,加速了离子和电荷传输,并赋予了优异的电化学活性,包括高比容量和稳定的循环性能。更重要的是,异质界面处硒化镍(101)面和硒化钼(100)面的晶格间距与氧化锂(100)面高度匹配,有利于氧化锂的外延生长以及循环过程中放电产物的形成和分解。这种采用非化学计量化合物构建异质结并改善锂氧电池性能的策略有望应用于其他能量存储或转换系统。

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